| Company Name: |
Alfa Chemistry |
| Tel: |
1-516-6625404 |
| Email: |
support@alfa-chemistry.com |
2-Linoleoyl-rac-glycerol manufacturers
|
| | 2-Linoleoyl-rac-glycerol Basic information |
| | 2-Linoleoyl-rac-glycerol Chemical Properties |
| Melting point | 9°C | | Boiling point | 485.0±40.0 °C(Predicted) | | density | 0.981±0.06 g/cm3(Predicted) | | Fp | 2℃ | | storage temp. | -20°C | | solubility | Chloroform (Slightly), DMF (Slightly), DMSO (Slightly), Ethyl Acetate (Slightly) | | pka | 13.54±0.10(Predicted) | | form | Oil | | color | Colourless to Pale Yellow | | BRN | 1715064 | | Stability: | Temperature Sensitive | | CAS DataBase Reference | 3443-82-1 |
| | 2-Linoleoyl-rac-glycerol Usage And Synthesis |
| Chemical Properties | Colourless Oil | | Uses | A fatty acid monoglycerides in vegetable oils with medium unsaturation. | | Uses | 2-Arachidonoyl glycerol (2-AG) has been isolated from porcine brain, and has been characterized as the natural endocannabinoid ligand for the CB1 receptor. The congener of 2-AG in which a linoleoyl group replaces the arachidonoyl group is 2-linoleoyl glycerol (2-LG), and this compound also appears in vivo in conjunction with 2-AG. Although the intrinsic activity of 2-LG is low, it potentiates the activity of other endocannabinoids, including 2-AG. This “entourage” effect has been attributed to blockade of the breakdown and reuptake pathways that normally function to reduce endocannabinoid levels rapidly upon release. | | Definition | ChEBI: A 2-monoglyceride where linoleoyl forms the 2-acyl group. |
| | 2-Linoleoyl-rac-glycerol Preparation Products And Raw materials |
|